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9CHV

cryo-EM structure of calcineurin-fused beta2 adrenergic receptor in apo state

Functional Information from GO Data
ChainGOidnamespacecontents
A0001569biological_processbranching involved in blood vessel morphogenesis
A0001837biological_processepithelial to mesenchymal transition
A0004721molecular_functionphosphoprotein phosphatase activity
A0004723molecular_functioncalcium-dependent protein serine/threonine phosphatase activity
A0004930molecular_functionG protein-coupled receptor activity
A0004935molecular_functionadrenergic receptor activity
A0004941molecular_functionbeta2-adrenergic receptor activity
A0005509molecular_functioncalcium ion binding
A0005515molecular_functionprotein binding
A0005516molecular_functioncalmodulin binding
A0005654cellular_componentnucleoplasm
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0005886cellular_componentplasma membrane
A0005955cellular_componentcalcineurin complex
A0006606biological_processprotein import into nucleus
A0006940biological_processregulation of smooth muscle contraction
A0007186biological_processG protein-coupled receptor signaling pathway
A0007189biological_processadenylate cyclase-activating G protein-coupled receptor signaling pathway
A0007507biological_processheart development
A0008287cellular_componentprotein serine/threonine phosphatase complex
A0008597molecular_functioncalcium-dependent protein serine/threonine phosphatase regulator activity
A0014044biological_processSchwann cell development
A0016020cellular_componentmembrane
A0019902molecular_functionphosphatase binding
A0019904molecular_functionprotein domain specific binding
A0022011biological_processmyelination in peripheral nervous system
A0033173biological_processcalcineurin-NFAT signaling cascade
A0034504biological_processprotein localization to nucleus
A0042383cellular_componentsarcolemma
A0045202cellular_componentsynapse
A0045944biological_processpositive regulation of transcription by RNA polymerase II
A0046872molecular_functionmetal ion binding
A0060487biological_processlung epithelial cell differentiation
A0070886biological_processpositive regulation of calcineurin-NFAT signaling cascade
A0097746biological_processblood vessel diameter maintenance
A0098685cellular_componentSchaffer collateral - CA1 synapse
A0098686cellular_componenthippocampal mossy fiber to CA3 synapse
A0098688cellular_componentparallel fiber to Purkinje cell synapse
A0098693biological_processregulation of synaptic vesicle cycle
A0098794cellular_componentpostsynapse
A0098978cellular_componentglutamatergic synapse
A0099149biological_processregulation of postsynaptic neurotransmitter receptor internalization
A0099170biological_processpostsynaptic modulation of chemical synaptic transmission
A1905665biological_processpositive regulation of calcium ion import across plasma membrane
A1905949biological_processnegative regulation of calcium ion import across plasma membrane
B0016787molecular_functionhydrolase activity
B0033192molecular_functioncalmodulin-dependent protein phosphatase activity
B0097720biological_processcalcineurin-mediated signaling
C0003007biological_processheart morphogenesis
C0003755molecular_functionpeptidyl-prolyl cis-trans isomerase activity
C0005160molecular_functiontransforming growth factor beta receptor binding
C0005246molecular_functioncalcium channel regulator activity
C0005515molecular_functionprotein binding
C0005527molecular_functionmacrolide binding
C0005528molecular_functionFK506 binding
C0005737cellular_componentcytoplasm
C0005829cellular_componentcytosol
C0006457biological_processprotein folding
C0006458biological_process'de novo' protein folding
C0010881biological_processregulation of cardiac muscle contraction by regulation of the release of sequestered calcium ion
C0014802cellular_componentterminal cisterna
C0014809biological_processregulation of skeletal muscle contraction by regulation of release of sequestered calcium ion
C0016020cellular_componentmembrane
C0016529cellular_componentsarcoplasmic reticulum
C0016853molecular_functionisomerase activity
C0030018cellular_componentZ disc
C0030512biological_processnegative regulation of transforming growth factor beta receptor signaling pathway
C0030547molecular_functionsignaling receptor inhibitor activity
C0032880biological_processregulation of protein localization
C0032926biological_processnegative regulation of activin receptor signaling pathway
C0033017cellular_componentsarcoplasmic reticulum membrane
C0034713molecular_functiontype I transforming growth factor beta receptor binding
C0042026biological_processprotein refolding
C0042110biological_processT cell activation
C0043123biological_processpositive regulation of canonical NF-kappaB signal transduction
C0044325molecular_functiontransmembrane transporter binding
C0050776biological_processregulation of immune response
C0051604biological_processprotein maturation
C0055010biological_processventricular cardiac muscle tissue morphogenesis
C0060347biological_processheart trabecula formation
C0070411molecular_functionI-SMAD binding
C0070697molecular_functionactivin receptor binding
C0097435biological_processsupramolecular fiber organization
C0098562cellular_componentcytoplasmic side of membrane
C1902991biological_processregulation of amyloid precursor protein catabolic process
C1990000biological_processamyloid fibril formation
C1990425cellular_componentryanodine receptor complex
Functional Information from PROSITE/UniProt
site_idPS00018
Number of Residues13
DetailsEF_HAND_1 EF-hand calcium-binding domain. DLDNSGSLSveEF
ChainResidueDetails
AASP246-PHE258
AASP278-PHE290
AASP315-LEU327
AASP356-PHE368

site_idPS00125
Number of Residues6
DetailsSER_THR_PHOSPHATASE Serine/threonine specific protein phosphatases signature. LRGNHE
ChainResidueDetails
BLEU146-GLU151

site_idPS00237
Number of Residues17
DetailsG_PROTEIN_RECEP_F1_1 G-protein coupled receptors family 1 signature. ASIeTLCVIAVDRYFaI
ChainResidueDetails
AALA119-ILE135

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues1
DetailsMOD_RES: N6-succinyllysine; alternate => ECO:0000250|UniProtKB:P26883
ChainResidueDetails
CLYS52

site_idSWS_FT_FI2
Number of Residues6
DetailsBINDING: BINDING => ECO:0000269|PubMed:26794871, ECO:0007744|PDB:4ORB
ChainResidueDetails
BASP89
BHIS91
BASP117
BASN149
BHIS198
BHIS280

site_idSWS_FT_FI3
Number of Residues1
DetailsSITE: Interaction with PxVP motif in substrate => ECO:0000250|UniProtKB:Q08209
ChainResidueDetails
BTRP351

site_idSWS_FT_FI4
Number of Residues1
DetailsMOD_RES: N-acetylserine => ECO:0000250|UniProtKB:Q08209
ChainResidueDetails
BSER1
AARG175-ASN196
AGLN422-LYS428

site_idSWS_FT_FI5
Number of Residues1
DetailsMOD_RES: 3'-nitrotyrosine => ECO:0007744|PubMed:16800626
ChainResidueDetails
BTYR223

site_idSWS_FT_FI6
Number of Residues23
DetailsTRANSMEM: Helical; Name=4
ChainResidueDetails
AARG151-TYR174

site_idSWS_FT_FI7
Number of Residues23
DetailsTRANSMEM: Helical; Name=5
ChainResidueDetails
AGLN197-SER220

site_idSWS_FT_FI8
Number of Residues23
DetailsTRANSMEM: Helical; Name=6
ChainResidueDetails
ALEU398-ILE421

site_idSWS_FT_FI9
Number of Residues23
DetailsTRANSMEM: Helical; Name=7
ChainResidueDetails
AGLU429-SER452

site_idSWS_FT_FI10
Number of Residues5
DetailsBINDING: BINDING => ECO:0000269|PubMed:18547522, ECO:0007744|PDB:3D4S
ChainResidueDetails
AASP113
ATHR118
AASN416
AASN435
ATYR439

site_idSWS_FT_FI11
Number of Residues1
DetailsBINDING: BINDING => ECO:0000269|PubMed:17952055, ECO:0000269|PubMed:17962520, ECO:0007744|PDB:2RH1
ChainResidueDetails
ASER203

site_idSWS_FT_FI12
Number of Residues1
DetailsMOD_RES: Phosphotyrosine => ECO:0000269|PubMed:8521811
ChainResidueDetails
ATYR141

site_idSWS_FT_FI13
Number of Residues2
DetailsMOD_RES: Phosphoserine; by PKA => ECO:0000269|PubMed:11146000
ChainResidueDetails
AASP468
AASP469

site_idSWS_FT_FI14
Number of Residues1
DetailsLIPID: S-palmitoyl cysteine => ECO:0000269|PubMed:27481942
ChainResidueDetails
ACYS388

site_idSWS_FT_FI15
Number of Residues1
DetailsLIPID: S-palmitoyl cysteine => ECO:0000269|PubMed:17962520, ECO:0000269|PubMed:18547522, ECO:0000269|PubMed:2540197, ECO:0000269|PubMed:27481942
ChainResidueDetails
ACYS464

site_idSWS_FT_FI16
Number of Residues15
DetailsBINDING: BINDING => ECO:0000255|PROSITE-ProRule:PRU00448, ECO:0000269|PubMed:12218175, ECO:0000269|PubMed:12357034, ECO:0000269|PubMed:17498738, ECO:0000269|PubMed:22343722, ECO:0000269|PubMed:23468591, ECO:0000269|PubMed:26794871, ECO:0000269|PubMed:27974827, ECO:0000269|PubMed:8524402, ECO:0007744|PDB:1AUI, ECO:0007744|PDB:1M63, ECO:0007744|PDB:1MF8, ECO:0007744|PDB:2P6B, ECO:0007744|PDB:3LL8, ECO:0007744|PDB:4F0Z, ECO:0007744|PDB:4OR9, ECO:0007744|PDB:4ORA, ECO:0007744|PDB:4ORC, ECO:0007744|PDB:5SVE
ChainResidueDetails
AASP246
AGLU289
AASP356
AASP358
AASP360
AARG362
AGLU367
AASP248
ASER250
ASER252
AGLU257
AASP278
AASP280
AASN282
AGLU284

site_idSWS_FT_FI17
Number of Residues5
DetailsBINDING: BINDING => ECO:0000255|PROSITE-ProRule:PRU00448, ECO:0000269|PubMed:12218175, ECO:0000269|PubMed:12357034, ECO:0000269|PubMed:17498738, ECO:0000269|PubMed:22343722, ECO:0000269|PubMed:23468591, ECO:0000269|PubMed:26794871, ECO:0000269|PubMed:27974827, ECO:0000269|PubMed:31375679, ECO:0000269|PubMed:8524402, ECO:0000312|PDB:6NUC, ECO:0007744|PDB:1AUI, ECO:0007744|PDB:1M63, ECO:0007744|PDB:1MF8, ECO:0007744|PDB:2P6B, ECO:0007744|PDB:3LL8, ECO:0007744|PDB:4F0Z, ECO:0007744|PDB:4OR9, ECO:0007744|PDB:4ORA, ECO:0007744|PDB:4ORC, ECO:0007744|PDB:5SVE
ChainResidueDetails
AASP315
AASP317
AASP319
ATYR321
AGLU326

site_idSWS_FT_FI18
Number of Residues2
DetailsSITE: Interaction with PxVP motif in substrates of the catalytic subunit => ECO:0000269|PubMed:23468591
ChainResidueDetails
AMET333
AASN337

site_idSWS_FT_FI19
Number of Residues1
DetailsMOD_RES: Phosphotyrosine => ECO:0000250|UniProtKB:Q63810
ChainResidueDetails
ATYR321

Catalytic Information from CSA
site_idMCSA1
Number of Residues6
DetailsM-CSA 362
ChainResidueDetails
CTYR26electrostatic destabiliser, steric role
CPHE36electrostatic destabiliser, polar/non-polar interaction, steric role
CASP37electrostatic stabiliser, steric role
CILE56electrostatic stabiliser, steric role
CTYR82electrostatic stabiliser, steric role
CPHE99electrostatic destabiliser, polar/non-polar interaction, steric role

237735

PDB entries from 2025-06-18

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